gudid
Primary ID: S7001
STOCKERT 70 (UDI S7001)
Manufactured by Stockert GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for STOCKERT 70 - Primary ID S7001
Device Regulatory Overview
The STOCKERT 70 (Model/Catalog Number: S7001) is a medical device manufactured by Stockert GmbH. This product is indexed under FDA Product Code / Category Classification DRF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- S7001
- Product Code / EMDN
- DRF
- Device Name
- Database Sync Date
- 2026-08-09 09:17:35
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of STOCKERT 70?
The registered manufacturer of record for STOCKERT 70 is Stockert GmbH.
What is the Primary UDI-DI identifier for STOCKERT 70?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is S7001.
What classification code is assigned to this device?
This device is registered under product classification code DRF.
Similar Classification Devices (DRF)
Other Devices by Stockert GmbH
Programmatic Export
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